Canonical Allele Identifier: PA2828483482
Gene: USP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2305117
ClinVar RCV Id: RCV002895954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358326.1:p.Leu93Phe
CA3058868
NM_001371397.1:c.277C>T